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Dynamic Kinetic Resolution of α-Keto Esters via Asymmetric Transfer Hydrogenation

The dynamic kinetic resolution of β-aryl α-keto esters has been accomplished using a newly designed (arene)RuCl(monosulfonamide) transfer hydrogenation catalyst. This dynamic process generates three contiguous stereocenters with remarkable diastereoselectivity through a reduction/lactonization seque...

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Bibliografische gegevens
Hoofdauteurs: Steward, Kimberly M., Gentry, Emily C., Johnson, Jeffrey S.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 2012
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3342478/
https://ncbi.nlm.nih.gov/pubmed/22509806
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ja3027136
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